成功分阶段的手术治疗闭锁与尿道直肠瘘的雄性小猫。

IF 0.7 Q3 VETERINARY SCIENCES
Journal of Feline Medicine and Surgery Open Reports Pub Date : 2025-06-05 eCollection Date: 2025-01-01 DOI:10.1177/20551169251337835
Nithida Boonwittaya, Wutti Bunjerdsuwan, Piyathip Choochalermporn
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引用次数: 0

摘要

病例总结:一只2个月大的雄性英国短毛猫被怀疑患有肛门闭锁。体格检查发现肛门不穿孔,并有少量粪便通过阴茎排出。x线表现,连同逆行尿道造影,证实诊断为II型闭锁伴尿道直肠瘘。手术后患者恢复良好。8个月大时,先天性尿道直肠瘘经会阴单路手术治疗,包括经同一切口行瘘管切除术和去势。术后短期预后良好,排便和排尿正常。相关性和新信息:闭锁是一种罕见的先天性异常,特别是在公猫。尽管手术技术取得了进步,但该病例是首例成功分阶段手术治疗雄性小猫II型闭锁尿道直肠瘘的病例,可能影响未来类似先天性异常的手术入路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful staged surgical management of atresia ani with urethrorectal fistula in a male kitten.

Case summary: A 2-month-old male British Shorthair cat was referred with suspected atresia ani. Physical examination revealed an imperforate anus and dribbling of faecal discharge through the penis. Radiographic findings, along with a retrograde urethrogram, confirmed the diagnosis of type II atresia ani with a urethrorectal fistula. Surgical anoplasty was performed and the patient recovered well. At 8 months of age, surgical treatment for the congenital urethrorectal fistula was carried out via a single perineal approach, including fistulectomy and castration through the same incision. Postoperative short-term outcomes were excellent, with normal defecation and urination.

Relevance and novel information: Atresia ani is a rare congenital anomaly, particularly in male cats. Despite advancements in surgical techniques, this case represents the first successful staged surgical management of urethrorectal fistula with type II atresia ani in a male kitten, potentially influencing future surgical approaches for similar congenital anomalies.

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来源期刊
CiteScore
1.30
自引率
14.30%
发文量
57
审稿时长
15 weeks
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